EP2130435B1 - Mittel zur erhöhung der alkaliresistenz von pflanzen sowie verfahren zur erhöhung der alkaliresistenz von pflanzen - Google Patents

Mittel zur erhöhung der alkaliresistenz von pflanzen sowie verfahren zur erhöhung der alkaliresistenz von pflanzen Download PDF

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Publication number
EP2130435B1
EP2130435B1 EP08720659.5A EP08720659A EP2130435B1 EP 2130435 B1 EP2130435 B1 EP 2130435B1 EP 08720659 A EP08720659 A EP 08720659A EP 2130435 B1 EP2130435 B1 EP 2130435B1
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Prior art keywords
iron
agent
plant
group
soil
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EP08720659.5A
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French (fr)
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EP2130435B8 (de
EP2130435A4 (de
EP2130435A1 (de
Inventor
Keitaro Watanabe
Toshihiro Kobori
Tohru Tanaka
Kazuya Iwai
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Cosmo Ala Co Ltd
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Cosmo Oil Co Ltd
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    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
    • A01N59/16—Heavy metals; Compounds thereof
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds

Definitions

  • the present invention relates to an agent for improving alkali tolerance of a plant, and to a method for improving alkali tolerance of a plant through treatment with the agent.
  • 5-aminolevulinic acid, a derivative thereof, and a salt of either of these are known to promote plant growth and to improve cold resistance (Patent Document 1), and also to improve plant growth under low-luminance conditions (Patent Document 2). Also known is a technique of improving salt tolerance of plant by use of these compounds for solving the problem of poor soil (Patent Document 3). Furthermore, spraying of 5-aminolevulinic acid is known to prevent decrease in foliage yield of plants grown in alkaline soil (Non-Patent Document 1). Yoshida et al. The Hokuriku Crop Science, no.
  • an object of the present invention is to provide an agent and a method for improving alkali tolerance of plant.
  • Non-Document 1 discloses spraying of 5-aminolevulinic acid in combination with an iron chelate. According to the disclosure, the foliage yield of plant in the combined spray area is lower than that in a water-treated area without spraying thereof, indicating that spraying the two species in combination exhibits no effect on improvement of alkali tolerance.
  • the present inventors have carried out extensive studies on alkali damage to plants, and have found that a combination of 5-aminolevulinic acid, a derivative thereof, or a salt of either of these with a specific amount of an iron compound remarkably improves alkali tolerance of a plant grown in strongly alkaline soil.
  • the present inventors have also found that the alkali tolerance is further improved through further adding elemental sulfur to the combination.
  • the present invention has been accomplished on the basis of these findings.
  • the present invention provides an agent for improving alkali tolerance of a plant, comprising:
  • the present invention also provides a method for improving alkali tolerance of a plant, characterized by treating a plant, or soil or a medium in which the plant grows with the agent for improving alkali tolerance of a plant.
  • alkali tolerance of a plant can be improved, whereby agricultural production in strongly alkaline soil and greening of alkaline soil can be realized.
  • alkaline conditions refers to conditions where a plant is damaged with alkali.
  • the soil under the conditions is referred to as “alkaline soil.”
  • alkaline soil the definition of alkaline soil is varied in accordance with the type of plant, and the alkaline soil is not defined strictly by the pH of the soil.
  • alkaline soil soil having a pH of 7 or higher, under which many plants are damaged, is called “alkaline soil,” and that having a pH of 8 or higher, particularly 8.5 or higher, is called “strongly alkaline soil.”
  • the agent for improving alkali tolerance of the present invention exhibits a remarkable effect at a pH of 7 or higher, preferably 7.5 or higher, more preferably 8 or higher, still more preferably 8.5 or higher, particularly preferably 8.8 or higher.
  • the upper limit of the pH is preferably 13.
  • alkaline conditions cannot be determined for all the plants. For the sake of understanding the concept of "alkaline conditions,” some examples will be given below.
  • Spinach is an alkalophilic plant, and the optimum pH of the soil for growth thereof is about 7.5. Although the soil having such a pH is "alkaline soil" for many plants, spinach grows most vitally at that pH. However, when the pH of the soil is in excess of 8, the growth of spinach is considerably impaired, resulting in diminishing green color of foliage. That is, the alkaline soil for spinach has a pH of 8 or higher, which is higher than the alkaline pH for many plants.
  • Blueberry is an acidophilic plant, and the optimum pH of the soil for growth thereof is about 5.5. Blueberry is alkali-damaged even in soil having a pH of 6.5, which is preferred for many plants, and suppression of growth and yellowing of foliage are observed. That is, the alkaline soil for blueberry has a pH of 6.5 or higher, which is lower than the pH for many plants.
  • the 5-aminolevulinic acid or a derivative thereof are compounds represented by formula (1): [F1] R 2 R 1 NCH 2 COCH 2 CH 2 COR 3 (1) (wherein each of R 1 and R 2 represents a hydrogen atom, an alkyl group, an acyl group, an alkoxycarbonyl group, an aryl group, or an aralkyl group, and R 3 represents a hydroxy group, an alkoxy group, an acyloxy group, an alkoxycarbonyloxy group, an aryloxy group, an aralkyloxy group, or an amino group), or a salt thereof.
  • the alkyl group (R 1 and R 2 ) is preferably a C1 to C24 linear or branched alkyl group, more preferably a C1 to C18 alkyl group, particularly preferably a C1 to C6 alkyl group.
  • the C1 to C6 alkyl group include methyl, ethyl, n-propyl, isopropyl, n-butyl, and secbutyl.
  • the acyl group is preferably a C1 to C12 linear or branched alkanoyl group, alkenylcarbonyl group, or aroyl group, particularly preferably a C1 to C6 alkanoyl group.
  • the acyl group examples include formyl, acetyl, propionyl, and butyryl.
  • the alkoxycarbonyl group is preferably a C2 to C13 (in total) alkoxycarbonyl group, particularly preferably C2 to C7 alkoxycarbonyl group.
  • Examples of the alkoxycarbonyl group include methoxycarbonyl, ethoxycarbonyl, n-propoxycarbonyl, and isopropoxycarbonyl.
  • the aryl group is preferably a C6 to C16 aryl group, for example, phenyl or naphthyl.
  • the aralkyl group is preferably a group formed from a C6 to C16 aryl group and the aforementioned C1 to C6 alkyl group, for example, benzyl.
  • the alkoxy group (R 3 in formula (1)) is preferably a C1 to C24 linear or branched alkoxy group, more preferably a C1 to C16 alkoxy group, particularly preferably a C1 to C12 alkoxy group.
  • Examples of the alkoxy group include methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, pentyloxy, hexyloxy, octyloxy, decyloxy, and dodecyloxy.
  • the acyloxy group is preferably a C1 to C12 linear or branched alkanoyloxy group, particularly preferably a C1 to C6 alkanoyloxy group.
  • the acyloxy group examples include acetoxy, propionyloxy, and butyryloxy.
  • the alkoxycarbonyloxy group is preferably a C2 to C13 (in total) alkoxycarbonyloxy group, particularly preferably a C2 to C7 (in total) alkoxycarbonyloxy group.
  • Examples of the alkoxycarbonyloxy group include methoxycarbonyloxy, ethoxycarbonyloxy, n-propoxycarbonyloxy, and isopropoxycarbonyloxy.
  • the aryloxy group is preferably a C6 to C16 aryloxy group, for example, phenoxy or naphthyloxy.
  • the aralkyloxy group is preferably a group including the aforementioned aralkyl group, for example, benzyloxy.
  • each of R 1 and R 2 is preferably a hydrogen atom.
  • R 3 is preferably a hydroxy group, an alkoxy group, or an aralkyloxy group, more preferably a hydroxy group or a C1 to C12 alkoxy group, particularly preferably methoxy or hexyloxy.
  • Examples of the 5-aminolevulinic acid derivative include 5-aminolevulinic acid methyl ester, 5-aminolevulinic acid ethyl ester, 5-aminolevulinic acid propyl ester, 5-aminolevulinic acid butyl ester, 5-aminolevulinic acid pentyl ester, and 5-aminolevulinic acid hexyl ester. Of these, 5-aminolevulinic acid methyl ester and 5-aminolevulinic acid hexyl ester are particularly preferred.
  • the salt of 5-aminolevulinic acid or the salt of a derivative thereof is particularly preferably 5-aminolevulinic acid hydrochloride or 5-aminolevulinic acid phosphate.
  • salts may be produced through any of the chemical synthesis methods and methods employing a microorganism or an enzyme.
  • the salts may be produced through methods disclosed in JP-A-1973-92328 , JP-A-1987-111954 , JP-A-1990-76841 , JP-A-1994-172281 , JP-A-1995-188133 , JP-A-1999-42083 , etc.
  • the thus-produced 5-aminolevulinic acid, a salt thereof, a derivative of either of these, and a reaction mixture and fermentation liquid thereof before purification may be employed without separation and purification, so long as they is not harmful for plant.
  • commercial products of the salts may be employed.
  • 5-aminolevulinic acid a derivative thereof, and a salt of either of these may be used singly or in combination of two or more species.
  • iron compound employed in the present invention No particular limitation is imposed on the iron compound employed in the present invention, so long as the compound contains iron and is not harmful for plants.
  • Specific example include metallic iron, iron salts, and iron chelates.
  • the salts include organic acid salts and inorganic acid salts.
  • the organic acid include carboxylic acids such as hydroxycarboxylic acids.
  • the carboxylic acid include those having carbon atoms in total of 2 to 8.
  • iron chelate examples include the compounds represented by formula (2): (wherein each of m1, m2, m3, and m4 is a number of 1 to 4; each of R 4 , R 5 , R 6 , and R 7 represents -COO - or -SO 3 - ; A represents -(CH 2 ) m5 - or -(CH 2 ) m6 -N[-(CH 2 ) m7 -R 8 ]-(CH 2 ) m8 - (wherein each of m5, m6, m7, and m8 is a number of 1 to 4, and R 8 represents -COO - or -SO 3 - ); p is a number of 2 or 3; q is a number of 1 to 3; r is a number of 0 to 2; and L represents NH 4 or an alkali metal, wherein when A represents -(CH 2 ) m5 -, p+q+r is 4, and when A represents (CH)
  • each of R 4 , R 5 , R 6 , and R 7 is preferably -COO - .
  • each of m1, m2, m3, and m4 is preferably 1.
  • A represents - (CH 2 ) m5 -, and p is 3, q is 1, and r is 0. More preferably m5 is 2 or 3.
  • A represents -(CH 2 ) m6 -N[-(CH 2 ) m7 -R 8 ]-(CH 2 ) m8 -, and p is 3, q is 1, and r is 1. More preferably, each of m6, m7, and m8 is 1 or 2, R 8 is -COO - , and L is NH 4 .
  • iron compound employed in the present invention examples include metallic iron, iron oxide, heme iron, iron citrate, iron succinate, iron sodium citrate, iron ammonium citrate, iron acetate, iron oxalate, iron malate, iron sodium succinate citrate, ferrous pyrophosphate, ferric pyrophosphate, dextran iron, iron lactate, iron gluconate, sodium ethylenediaminetetraacetatoferrate, potassium ethylenediaminetetraacetatoferrate, ammonium ethylenediaminetetraacetatoferrate, sodium diethylenetriaminepentaacetatoferrate, potassium diethylenetriaminepentaacetatoferrate, ammonium diethylenetriaminepentaacetatoferrate, iron fulvate, iron humate, iron ligninsulfate, iron chloride, iron nitrate, iron sulfate, ammonium iron sulfate, iron glycerophosphate, iron tartrate, and iron glyco
  • the ratio of the concentration of 5-aminolevulinic acid, a derivative thereof, or a salt of either of these to the concentration of iron compound which varies depending on the use of the agent, is 1 to 10,000 mass% (iron compound, as reduced to iron) with respect to 100 mass% of 5-aminolevulinic acid, a derivative thereof, or a salt of either of these.
  • the ratio is preferably 20 to 1,000 mass%, more preferably 50 to 1,000 mass%, still more preferably 50 to 300 mass%, particularly preferably 80 to 200 mass%, with respect to 100 mass% of 5-aminolevulinic acid, a derivative thereof, or a salt of either of these.
  • elemental sulfur is incorporated into the agent for improving alkali tolerance of the present invention.
  • the term "elemental sulfur” refers to a substance consisting of exclusively of sulfur atoms (e.g., S8, S6, S4, and S2, and the like), and the form thereof is not particularly limited. Specifically, elemental sulfur which is also commercially available as a pharmaceutical product as defined by Pharmacopoeia of Japan may be used. In the present invention, a mixture of S8, S6, and the like may be used, so long as it is generally available, and the purity of such products is not particularly limited. The form thereof may be brains or powder, so long as it is solid. No particular limitation is imposed on the particle size, and the particle size is preferably 0.001 to 10 mm, more preferably 0.01 to 5 mm, particularly preferably 0.01 to 3 mm.
  • the ratio (by mass) of the concentration of 5-aminolevulinic acid, a derivative thereof, or a salt of either of these to the concentration of elemental sulfur, which varies depending on the use of the agent, is 100 to 10,000,000, preferably 1,000 to 1,000,000, more preferably 5,000 to 1,000,000, with respect to 1 part by mass of 5-aminolevulinic acid, a derivative thereof, or a salt of either of these.
  • the agent for improving alkali tolerance of the present invention may further contain additional ingredients such as an agent for regulating plant growth, saccharide, amino acid, nucleic acid, organic acid, alcohol, vitamin, sulfur species other than elemental sulfur, mineral, and the like.
  • Examples of the agent for regulating plant growth include brassinolide such as epibrassinolide, cholines such as choline chloride and choline nitrate, indolebutyric acid, indoleacetic acid, ethychlozate, 1-naphthylacetamide, isoprothiolane, nicotinamide, hydroxyisoxazole, calcium peroxide, benzylaminopurine, methasulfocarb, oxyethylene docosanol, ethephon, cloxyfonac, gibberellin, streptomycin, daminozide, benzylaminopurine, 4-CPA, ancymidol, inabenfide, uniconazole, chlormequat, dikegulac, mefluidide, calcium carbonate, and piperonyl butoxide.
  • brassinolide such as epibrassinolide
  • cholines such as choline chloride and
  • saccharide examples include glucose, xylitol, sorbitol, galactose, xylose, mannose, arabinose, madulose, sucrose, ribose, rhamnose, fructose, maltose, lactose, and maltotriose.
  • amino acid examples include asparagine, glutamine, histidine, tyrosine, glycine, arginine, alanine, tryptophan, methionine, valine, proline, leucine, lysine, isoleucine, and ectoine.
  • nucleic acid examples include RNA and DNA.
  • organic acid examples include formic acid, acetic acid, propionic acid, butyric acid, valeric acid, oxalic acid, phthalic acid, benzoic acid, lactic acid, citric acid, tartaric acid, malonic acid, malic acid, succinic acid, glycolic acid, glutamic acid, aspartic acid, maleic acid, caproic acid, caprylic acid, myristic acid, stearic acid, palmitic acid, pyruvic acid, ⁇ -ketoglutaric acid, and levulinic acid.
  • Examples of the alcohol include methanol, ethanol, propanol, butanol, pentanol, hexanol, and glycerol.
  • vitamin examples include nicotinamide, vitamin B6, vitamin B12, vitamin B5, vitamin C, vitamin B13, vitamin B1, vitamin B3, vitamin B2, vitamin K3, vitamin A, vitamin D2, vitamin D3, vitamin K1, ⁇ -tocopherol, ⁇ -tocopherol, ⁇ -tocopherol, p-hydroxybenzoic acid, biotin, folic acid, nicotinic acid, pantothenic acid, and ⁇ -liponic acid.
  • sulfur species other than elemental sulfur examples include sulfuric acid, sulfurous acid, thiosulfuric acid, hydrogensulfate, hydrogensulfite, and sulfonic acid.
  • Examples of the mineral include nitrogen, phosphoric acid, potassium, boron, manganese, magnesium, zinc, copper, and molybdenum.
  • the agent for improving alkali tolerance of the present invention may be in any forms such as powder, granules, liquid, and a flowable agent. These forms may be prepared by a conventional method by use of an additive such as a solvent, a dispersant, or an extender. In the agent for improving alkali tolerance of the present invention containing elemental sulfur, solid forms such as powder and granules are preferred.
  • No particular limitation is imposed on the plant to which the agent for improving alkali tolerance of the present invention is applied.
  • the plant include grains, vegetables, fruits, flowing plants, arbores, luguminia, lawn grass, potatoes, allium, and pasturage.
  • Curciferae such as Komatsuna
  • Malvaceae such as cotton
  • true grasses such as corn
  • Compositae such as sunflower
  • Solanaceae such as tomato.
  • More specific examples include soybean, kidney bean, broad bean, Chinese cabbage, perilla, Festuca pratensis Huds, Phalaris arundinacea L., Alsike clover, white clover, ladino clover, Pangola grass, colored guinea grass, guinea grass, Dallis grass, green leaf desmodium, Pueraria hirsuta, onion, aspapagus, peas, cabbage, brown mustard, carrot, garland chrysanthemum, red clover, crimson clover, chinese milk vetch, rose grass, green panic, barley, soughum, Mizuna, sponge gourd, beats, spinach, eggplant, capsicum, lettuce, burdock, alfalfa, Buffel grass, foxtail millet,
  • Acidophilic plants receive alkali-stress even in ordinary soil. Therefore, such stress is often observed not only in alkaline soil but also in ordinary soil.
  • Examples of such plants include rice, oat, rye, buckwheat, tea, cranberry, orchard grass, Festuca araundinacea, Italian rye grass, talloat grass, bird's foot trefoil, hagi, Bermuda grass, molasses grass, miles lotononis, styro, wheat, corn, sawa millet, hog millet, radish, rutabaga, weeping love grass, Bahia grass, Nepier grass, Centrosema pubescens, blueberry, apple, rhododendron, azalea, gardenia, begonia, maidenhair, nephrolepis, ananas, lily of the valley, ageratum, calla lily, and clematis.
  • the agent for improving alkali tolerance of the present invention may be applied to a plant in foliage treatment (as a foliage treatment agent), soil treatment (as a soil treatment agent), or aerosol treatment (as an aerosol treatment agent).
  • foliage treatment as a foliage treatment agent
  • soil treatment as a soil treatment agent
  • aerosol treatment as an aerosol treatment agent
  • the agent for improving alkali tolerance of the present invention containing elemental sulfur is applied to a plant
  • the agent is preferably applied in soil treatment (soil treatment agent).
  • the agent of the present invention may be absorbed by a plant before planting, cutting, etc. of the plant.
  • the agent may be added to water for hydroponic culture.
  • the agent for improving alkali tolerance of the present invention may be applied a plurality of times to a plant, or to soil or a medium in which the plant grows.
  • the ingredients, 5-aminolevulinic acid, a derivative thereof, a salt of either of these, an iron compound, and elemental sulfur may be applied separately. In this case, the same application method or different methods may be employed. No particular limitation is imposed on the sequence and intervals of application of the agent for improving alkali tolerance and elemental sulfur, and each ingredient may be applied a plurality of times.
  • the amount of ingredients is on the basis of 5-aminolevulinic acid or a similar compound, an iron compound and, furthermore, elemental sulfur are preferably used at the aforementioned proportions.
  • the agent for improving alkali tolerance of the present invention is used as a foliage treatment agent
  • 5-aminolevulinic acid, a derivative thereof, or a salt of either of these is added to a solvent at a concentration of 0.1 to 1,000 ppm, preferably 0.5 to 500 ppm, more preferably 0.5 to 300 ppm, and the thus-obtained liquid agent is used 10 to 1,000 L per 10 ares, more preferably 50 to 300 L.
  • a wetting agent is preferably used in combination. No particular limitation is imposed on the type and amount of the wetting agent.
  • the agent for improving alkali tolerance of the present invention is used as a soil treatment agent
  • the agent (as 5-aminolevulinic acid, a derivative thereof, or a salt of either of these) is preferably used 1 to 1,000 g per 10 ares, more preferably 10 to 500 g. In the case of hydroponic culture, the amount is preferably a half thereof.
  • the agent for improving alkali tolerance of the present invention is used as an aerosol treatment agent
  • the agent (as 5-aminolevulinic acid, a derivative thereof, or a salt of either of these) is added to a solvent at a concentration of 0.1 to 1,000 ppm, preferably 0.5 to 500 ppm, and the thus-obtained liquid agent is used 10 to 1,000 L per 10 ares, more preferably 50 to 300 L.
  • the liquid of the agent for improving alkali tolerance of the present invention preferably has a concentration of 0.001 to 10 ppm, more preferably 0.01 to 5 ppm.
  • the immersion time is preferably one hour to one week, more preferably three hours to one day.
  • any of the above treatment methods is effective when it is performed in any phase of plant growth. Particularly, a remarkable effect can be attained when any treatment method is performed in a seedling state or a fruit maturity stage.
  • Each treatment method provides a sufficient effect by a single treatment. However, through performing any of the treatment methods a plurality of times, the effect is more enhanced. When treatment is performed a plurality of times, the aforementioned treatment methods may be combined.
  • the agent for improving alkali tolerance of the present invention is employed in a mixture with a pesticide, fertilizer, etc. for the purpose of convenience, any kind of material may be mixed with the agent, so long as the effect of the present invention is not impaired.
  • Each of the pots (1/5000 a) was filled with andosols soil, and Komatsuna (species: Calvita, product of Nohara Seed Co., Ltd.) was sown in the soil. At the 3 leaf stage, five uniform seedlings per pot were selected by cutting. An aqueous solution (0.05 wt.%) of each agent having a composition shown in Table 1 was applied to the stems and leaves of the plants in each pot (5 mL/pot). Sulfur powder ("sulfur, powder," product of Wako Pure Chemical Industries, Ltd.) was separately used in an amount given in Table 1 for soil treatment. The same sulfur powder was employed in the following Examples.
  • Table 1 shows the results.
  • water was employed instead of an aqueous solution of each agent.
  • Examples 1 to 5, 7, 8, 10, 11, 13, 15, 16, 17, 19, 21 and 23 are reference examples.
  • an aqueous solution (0.05 mass%) of each agent having a composition shown in Table 2 was sprayed every 2 weeks to the stems and leaves of the plants in each pot (5 mL/pot), and the pot was controlled under ordinary conditions. Twenty-seven days after sowing, the soil was washed out with water, whereby the plants were harvested. The plant height of each plant was measured. Subsequently, the plants were dried at 80°C for 24 hours by a drier, and the dry weight of shoots of each plant was measured.
  • Example 7 The test procedure of Example 7 was repeated, except that the amounts of ingredients were changed. The results are shown in Table 2.
  • Example 7 The test procedure of Example 7 was repeated, except that application of sulfur to soil treatment and application of other agent ingredients to foliage treatment were simultaneously performed. The results are shown in Table 2.
  • Example 7 The test procedure of Example 7 was repeated, except that no agent treatment was performed. The results are shown in Table 2.
  • Example 7 The test procedure of Example 7 was repeated, except that the agent was changed. The results are shown in Table 2.
  • Example 7 The test procedure of Example 7 was repeated, except that the agent was changed. The results are shown in Table 2.
  • Example 7 The test procedure of Example 7 was repeated, except that the agent was changed. The results are shown in Table 2.
  • Table 2 pH of soil Agent Plant height(cm) Dry weight of shoots (g) Ingredients Concentration (mass%) Ex. 7 8.8 5-Aminolevulinic acid hydrochloride 0.3 13.5 2.7 Fe-DTPA *3 0.6 *2 Ex. 8 8.8 5-Aminolevulinic acid hydrochloride 0.3 11.4 2.4 Fe-DTPA *3 0.06 *2 Ex. 9 8.8 5-Aminolevulinic acid hydrochloride 0.3 14.6 3.5 Fe-DTPA *3 0.6 *2 Sulfur powder 0.25 g Comp. Ex. 4 8.8 (No treatment) - 10.2 2.1 Comp. Ex.
  • Example 7 The test procedure of Example 7 was repeated, except that soil (pH of 7.6) was prepared. The results are shown in Table 3.
  • Example 10 The test procedure of Example 10 was repeated, except that the amounts of ingredients were changed. The results are shown in Table 3.
  • Example 10 The test procedure of Example 10 was repeated, except that application of sulfur to soil treatment and application of other agent ingredients to foliage treatment were simultaneously performed. The results are shown in Table 3.
  • Example 10 The test procedure of Example 10 was repeated, except that no agent treatment was performed. The results are shown in Table 3.
  • Table 3 pH of soil Agent Plant height(cm) Dry weight of shoots(g) Ingredients Concentration (mass%) Ex. 10 7.6 5-Aminolevulinic acid hydrochloride 0.3 20.5 3.6 Fe-DTPA *3 0.6 *2 Ex. 11 7.6 5-Aminolevulinic acid hydrochloride 0.3 20.0 3.5 Fe-DTPA *3 0.06 *2 Ex. 12 7.6 5-Aminolevulinic acid hydrochloride 0.3 22.0 4.1 Fe-DTPA *3 0.6 *2 Sulfur powder 0.25 g Comp. Ex. 8 7.6 (No treatment) - 17.1 3.2 *2: In iron equivalent *3: Ammonium diethylenetriaminepentaacetatoferrate
  • an aqueous solution (0.05 mass%) of each agent having a composition shown in Table 4 was sprayed every 2 weeks to the stems and leaves of the plants in each pot (5 mL/pot), and the pot was controlled under ordinary conditions.
  • the soil was washed out with water, whereby the plants were harvested, and the plant height of each plant was measured. Subsequently, the plants were dried at 80°C for 24 hours by a drier, and the dry weight of shoots of each plant was measured.
  • Example 13 The test procedure of Example 13 was repeated, except that sulfur was further applied to soil treatment one day after foliage treatment with other agent ingredients. The results are shown in Table 4.
  • Example 13 The test procedure of Example 13 was repeated, except that no agent treatment was performed. The results are shown in Table 4.
  • Example 13 The test procedure of Example 13 was repeated, except that the agent was changed. The results are shown in Table 4.
  • Example 14 The test procedure of Example 13 was repeated, except that the agent was changed. The results are shown in Table 4.
  • Table 4 pH of soil Agent Plant height(cm) Dry weight of shoots(g) Ingredients Concentration (mass%)
  • Ex. 13 8.8 5-Aminolevulinic acid hydrochloride 0.3 16.3 1.4 Fe-DTPA *3 0.6 *2
  • Ex. 14 8.8 5-Aminolevulinic acid hydrochloride 0.3 18.1 1.7 Fe-DTPA *3 0.6 *2 Sulfur powder 0.25 g Comp. Ex. 9 8.8 (No treatment) - 12.8 0.7 Comp.
  • 10 8.8 5-Aminolevulinic acid hydrochloride 0.3 13.1 0.9 Comp.
  • Ex. 11 8.8 Sulfur powder 0.25 g 13.2 0.8 *2: In iron equivalent *3: Ammonium diethylenetriaminepentaacetatoferrate
  • Example 13 The test procedure of Example 13 was repeated, except that soil having a pH of 8.5 was prepared, and that the amounts of ingredients were changed. The results are shown in Table 5.
  • Example 15 The test procedure of Example 15 was repeated, except that the amounts of ingredients were changed. The results are shown in Table 5.
  • Example 15 The test procedure of Example 15 was repeated, except that no agent treatment was performed. The results are shown in Table 5.
  • Table 5 pH of soil Agent Plant height(cm) Dry weight of shoots(g) Ingredients Concentration (mass%) Ex. 15 8.5 5-Aminolevulinic acid hydrochloride 0.3 15.2 1.2 Fe-DTPA *3 0.3 *2 Ex. 16 8.5 5-Aminolevulinic acid hydrochloride 0.3 14.8 1.2 Fe-DTPA *3 0.15 *2 Comp. Ex. 12 8.5 (No treatment) - 13.1 0.7 *2: In iron equivalent *3: Ammonium diethylenetriaminepentaacetatoferrate
  • an aqueous solution (0.05 mass%) of each agent having a composition shown in Table 6 was sprayed every 2 weeks to the stems and leaves of the plants in each pot (5 mL/pot), and the pot was controlled under ordinary conditions.
  • the soil was washed out with water, whereby the plants were harvested, and the plant height of each plant was measured. Subsequently, the plants were dried at 80°C for 24 hours by a drier, and the dry weight of shoots of each plant was measured.
  • Example 17 The test procedure of Example 17 was repeated, except that application of sulfur to soil treatment and application of other agent ingredients to foliage treatment were simultaneously performed. The results are shown in Table 6.
  • Example 17 The test procedure of Example 17 was repeated, except that no agent treatment was performed. The results are shown in Table 6.
  • Example 17 The test procedure of Example 17 was repeated, except that the agent was changed. The results are shown in Table 6.
  • Example 17 The test procedure of Example 17 was repeated, except that the agent was changed. The results are shown in Table 6.
  • Table 6 pH of soil Agent Plant height(cm) Dry weight of shoots(g) Ingredients Concentration (mass%)
  • Ex. 17 8.7 5-Aminolevulinic acid hydrochloride 0.3 23.0 0.38 Fe-DTPA *3 0.6 *2
  • Ex. 18 8.7 5-Aminolevulinic acid hydrochloride 0.3 25.1 0.43 Fe-DTPA *3 0.6 *2 Sulfur powder 0.25 g Comp. Ex. 13 8.7 (No treatment) - 23.2 0.28 Comp. Ex. 14 8.7 5-Aminolevulinic acid hydrochloride 0.3 23.2 0.30 Comp.
  • Ex. 15 8.7 Sulfur powder 0.25 g 23.2 0.31 *2: In iron equivalent *3: Ammonium diethylenetriaminepentaacetatoferrate
  • Example 19 The test procedure of Example 19 was repeated, except that application of sulfur to soil treatment and application of other agent ingredients to foliage treatment were simultaneously performed. The results are shown in Table 7.
  • Example 19 The test procedure of Example 19 was repeated, except that no agent treatment was performed. The results are shown in Table 7.
  • Example 19 The test procedure of Example 19 was repeated, except that the agent was changed. The results are shown in Table 7.
  • Example 19 The test procedure of Example 19 was repeated, except that the agent was changed. The results are shown in Table 7. [Table 7] pH of soil Agent Plant height(cm) Dry weight of shoots (g) Ingredients Concentration (mass%) Ex. 19 8.8 5-Aminolevulinic acid hydrochloride 0.3 42 8.1 Fe-DTPA *3 0.6 *2 Ex.20 8.8 5-Aminolevulinic acid hydrochloride 0.3 45 9.2 Fe-DTPA *3 0.6 *2 Sulfur powder 0.25 g Comp. Ex. 16 8.8 (No treatment) - 33 6.3 Comp. Ex. 17 8.8 5-Aminolevulinic acid hydrochloride 0.3 36 6.8 Comp. Ex. 18 8.8 Sulfur powder 0.25 g 34 6.5 *2: In iron equivalent *3: Ammonium diethylenetriaminepentaacetatoferrate
  • Example 21 The test procedure of Example 21 was repeated, except that application of sulfur to soil treatment and application of other agent ingredients to foliage treatment were simultaneously performed. The results are shown in Table 8.
  • Example 21 The test procedure of Example 21 was repeated, except that no agent treatment was performed. The results are shown in Table 8.
  • Example 21 The test procedure of Example 21 was repeated, except that the agent was changed. The results are shown in Table 8.
  • Example 21 The test procedure of Example 21 was repeated, except that the agent was changed. The results are shown in Table 8. [Table 8] pH of soil Agent Dry weight of shoots(g) Ingredients Concentration (mass%) Ex. 21 8.8 5-Aminolevulinic acid hydrochloride 0.3 6.9 Fe-DTPA *3 0.6 *2 Ex. 22 8.8 5-Aminolevulinic acid hydrochloride 0.3 7.5 Fe-DTPA *3 0.6 *2 Sulfur powder 0.25 g Comp. Ex. 19 8.8 (No treatment) - 3.1 Comp. Ex. 20 8.8 5-Aminolevulinic acid hydrochloride 0.3 4.5 Comp. Ex. 21 8.8 Sulfur powder 0.25 g 4.0 *2: In iron equivalent *3: Ammonium diethylenetriaminepentaacetatoferrate
  • an aqueous solution (0.05 mass%) of each agent having a composition shown in Table 9 was applied every 2 weeks to the surface of the soil in each pot (10 mL/pot), and the pot was controlled under ordinary conditions. Twenty-seven days after sowing, the soil was washed out with water, whereby the plants were harvested, and the plant height of each plant was measured. Subsequently, the plants were dried at 80°C for 24 hours by a drier, and the dry weight of shoots of each plant was measured. The averaged values and test conditions are shown in Table 9.
  • Example 23 The test procedure of Example 23 was repeated, except that application of sulfur to soil treatment and application of other agent ingredients to foliage treatment were simultaneously performed. The results are shown in Table 9.
  • Example 23 The test procedure of Example 23 was repeated, except that no agent treatment was performed. The results are shown in Table 9.
  • Example 23 The test procedure of Example 23 was repeated, except that the agent was changed. The results are shown in Table 9.
  • Example 23 The test procedure of Example 23 was repeated, except that the agent was changed. The results are shown in Table 9.
  • Example 23 The test procedure of Example 23 was repeated, except that the agent was changed. The results are shown in Table 9.
  • Table 9 pH of soil Agent Plant height(cm) Dry weight of shoots (g) Ingredients Concentration (mass%)
  • Ex. 23 8.8 5-Aminolevulinic acid hydrochloride 0.3 13.0 2.6 Fe-DTPA *3 0.6 *2
  • Ex. 24 8.8 5-Aminolevulinic acid hydrochloride 0.3 13.2 3.0 Fe-DTPA *3 0.6 *2 Sulfur powder 0.25 g Comp. Ex. 22 8.8 (No treatment) - 10.2 2.1 Comp. Ex. 23 8.8 5-Aminolevulinic acid hydrochloride 0.3 10.3 2.1 Comp. Ex. 24 8.8 Fe-DTPA *3 0.6 *2 10.1 1.9 Comp.
  • Ex. 25 8.8 Sulfur powder 0.25 g 10.3 2.2 *2: In iron equivalent *3: Ammonium diethylenetriaminepentaacetatoferrate

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Claims (4)

  1. Mittel zur Verbesserung der Alkalitoleranz einer Pflanze, umfassend:
    (i) 5-Aminolävulinsäure oder ein Derivat davon der folgenden Formel (1):

            R2R1NCH2COCH2CH2COR3     (1)

    worin jedes von R1 und R2 für ein Wasserstoffatom, eine Alkylgruppe, eine Acylgruppe, eine Alkoxycarbonylgruppe, eine Arylgruppe oder eine Aralkylgruppe steht und R3 für eine Hydroxygruppe, eine Alkoxygruppe, eine Acyloxygruppe, eine Alkoxycarbonyloxygruppe, eine Aryloxygruppe, eine Aralkyloxygruppe oder eine Aminogruppe steht, oder ein Salz von diesen;
    (ii) eine Eisenverbindung; und
    (iii) elementaren Schwefel.
  2. Das Mittel zur Verbesserung der Alkalitoleranz gemäß Anspruch 1, das eine Eisenverbindung in einer Menge von 20 bis 1.000 Gewichtsprozent an Eisenäquivalenten bezogen auf 100 Gewichtsteile von 5-Aminolävulinsäure, einem Derivat davon oder einem Salz von einem von diesen enthält.
  3. Das Mittel zur Verbesserung der Alkalitoleranz einer Pflanze gemäß Anspruch 1 oder 2, worin die Eisenverbindung eine oder mehrere ausgewählt aus metallischem Eisen, Eisenoxid, Hämeisen, Eisencitrat, Eisensuccinat, Eisen-Natrium-Citrat, Eisen-Ammonium-Citrat, Eisenacetat, Eisenoxalat, Eisenmalat, Eisen-Natrium-Succinat-Citrat, Eisen(II)pyrophosphat, Eisen(III)pyrophosphat, Dextran-Eisen, Eisenlactat, Eisengluconat, Natrium-Ethylendiamintetraessigsäureferrat, Kalium-Ethylendiamintetraessigsäureferrat, Ammonium-Ethylendiamintetraessigsäureferrat, Natrium-Ethylentriaminpentaessigsäureferrat, Kalium-Diethylentriaminpentaessigsäureferrat, Ammonium-Diethylentriaminpentaessigsäureferrat, Eisenfulvat, Eisenhumat, Eisen-Ligininsulfat, Eisenchlorid, Eisennitrat, Eisensulfat, Eisenammoniumsulfat, Eisenglycophosphat, Eisentartrat und Eisenglycolat ist.
  4. Verfahren zur Verbesserung der Alkalitoleranz einer Pflanze, umfassend Behandeln einer Pflanze oder von Boden oder einem Mediums, in dem die Pflanze wächst, mit dem Mittel zur Verbesserung der Alkalitoleranz einer Pflanze gemäß einem der Ansprüche 1 bis 3.
EP08720659.5A 2007-03-30 2008-03-28 Mittel zur erhöhung der alkaliresistenz von pflanzen sowie verfahren zur erhöhung der alkaliresistenz von pflanzen Not-in-force EP2130435B8 (de)

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AU2009247547B2 (en) * 2008-05-13 2013-10-10 Cosmo Trade & Service Co., Ltd. Agent for improving lawn grass qualities
US8722123B2 (en) 2008-05-22 2014-05-13 University Of Georgia Research Foundation, Inc. Antimicrobial composition and use as food treatment
WO2011115798A2 (en) * 2010-03-17 2011-09-22 University Of Georgia Research Foundation, Inc. Antimicrobial treatment for seeds and sprouts
ES2472667T3 (es) 2010-03-24 2014-07-02 Cognis Ip Management Gmbh Composiciones biocidas que comprenden glicerol(éter)fosfatos
CN102884154B (zh) * 2010-04-09 2016-04-13 巴斯夫欧洲公司 作为传热介质的具有改进粘度的流体硫
JP5771454B2 (ja) * 2010-06-22 2015-09-02 コスモ石油株式会社 ナス科植物の高温障害抑制剤
JP5909332B2 (ja) * 2010-07-05 2016-04-26 株式会社誠和 ５−アミノレブリン酸の補助剤及びその使用方法
EP2590909A4 (de) 2010-07-07 2018-01-24 Jianmin Zhang Zusammensetzungen und verfahren zur herstellung und verwendung dieser zusammensetzungen zur verbesserung eines bodens oder eines pflanzenwachstums sowie verbesserter boden, verbesserte pflanzen und/oder verbessertes saatgut
CN103140457B (zh) * 2010-09-30 2015-05-13 克斯莫石油株式会社 含5-氨基乙酰丙酸的固体肥料及其制造方法
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CN107736368A (zh) * 2017-09-13 2018-02-27 西南大学 5‑氨基乙酰丙酸与氯吡脲混合制剂用于种植羊草的用途
CN107721604A (zh) * 2017-11-10 2018-02-23 广西肥源生物科技有限公司 一种盐碱地土壤调理剂及其制备方法
UA127565C2 (uk) * 2018-07-14 2023-10-11 Арун Віттхал Савант Сільськогосподарська композиція
CN110402737A (zh) * 2019-07-10 2019-11-05 中国农业科学院郑州果树研究所 一种抗寒、耐盐碱性的葡萄砧木的选育方法
CN111296260B (zh) * 2020-03-02 2021-09-14 元成环境股份有限公司 一种提升盆栽香腮杜鹃品质的培育方法
CN111713408A (zh) * 2020-07-01 2020-09-29 中国农业科学院郑州果树研究所 一种耐碱性猕猴桃种质资源的鉴定方法
CN112273087A (zh) * 2020-10-30 2021-01-29 黑龙江八一农垦大学 一种大豆耐盐碱性的鉴定方法
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US20100035754A1 (en) 2010-02-11
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AU2008238787B2 (en) 2013-05-02
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WO2008126374A1 (ja) 2008-10-23
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